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SMILES: Clc1ccc2c(NCCN3C(=S)N(C(=O)C3=O)c3ccccc3Cl)ccnc2c1

InChI Key: InChIKey=NPBDUBFUHRFPDY-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50003684   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Histidine-rich protein PFHRP-II


(Plasmodium falciparum)
BDBM50003684
PNG
(CHEMBL466228)
Show SMILES Clc1ccc2c(NCCN3C(=S)N(C(=O)C3=O)c3ccccc3Cl)ccnc2c1
Show InChI InChI=1S/C20H14Cl2N4O2S/c21-12-5-6-13-15(7-8-23-16(13)11-12)24-9-10-25-18(27)19(28)26(20(25)29)17-4-2-1-3-14(17)22/h1-8,11H,9-10H2,(H,23,24)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 13n/an/an/an/an/an/a



Central Drug Research Institute

Curated by ChEMBL


Assay Description
Antiplasmodial activity as inhibition of beta-hematin against Plasmodium yoelii N67 infected Swiss mice (Mus musculus) erythrocytes


Bioorg Med Chem Lett 19: 2570-3 (2009)


Article DOI: 10.1016/j.bmcl.2009.03.026
BindingDB Entry DOI: 10.7270/Q2JD4Z8D
More data for this
Ligand-Target Pair